PMC Links for Gene (Select 5459) - PMC

Links from Gene

Items: 1 to 20 of 27

<< First< Prev

Page of 2

Select item 104006271.

Ramifications of POU4F3 variants associated with autosomal dominant hearing loss in various molecular aspects

Sang-Yeon Lee, Min Young Kim, Jin Hee Han, Sang Soo Park, Yejin Yun, Seung-Cheol Jee, Jae Joon Han, Jun Ho Lee, Heeyoung Seok, Byung Yoon Choi

Sci Rep. 2023; 13: 12584. Published online 2023 Aug 3. doi: 10.1038/s41598-023-38272-w

PMCID:: PMC10400627

Abstract Article PDF–2.5M

Select item 103259932.

Highly variable hearing loss due to POU4F3 (c.37del) is revealed by longitudinal, frequency specific analyses

Sushma Singh, Cindy Penney, Anne Griffin, Geoffrey Woodland, Salem Werdyani, Tammy A. Benteau, Nelly Abdelfatah, Jessica Squires, Beverly King, Jim Houston, Matthew J. Dyer, Nicole M. Roslin, Daniel Vincent, Pascale Marquis, Darren D. O’Rielly, Kathy Hodgkinson, Taylor Burt, Ashley Baker, Susan G. Stanton, Terry-Lynn Young

Eur J Hum Genet. 2023 Jul; 31(7): 815–823. Published online 2023 Apr 19. doi: 10.1038/s41431-023-01358-0

PMCID:: PMC10325993

Abstract Article PDF–1.8M

Select item 82385893.

A Missense POU4F3 Variant Associated with Autosomal Dominant Midfrequency Hearing Loss Alters Subnuclear Localization and Transcriptional Capabilities

Dan Bai, Xudong Zhang, Yu Li, Jing Ni, Kai Lan

Biomed Res Int. 2021; 2021: 5574136. Published online 2021 Jun 21. doi: 10.1155/2021/5574136

PMCID:: PMC8238589

Abstract Article PDF–1.0M

Select item 73496274.

Four Novel Variants in POU4F3 Cause Autosomal Dominant Nonsyndromic Hearing Loss

Tian-Yi Cui, Xue Gao, Sha-Sha Huang, Yan-Yan Sun, Si-Qi Zhang, Xin-Xia Jiang, Yan-Zhong Yang, Dong-Yang Kang, Qing-Wen Zhu, Yong-Yi Yuan

Neural Plast. 2020; 2020: 6137083. Published online 2020 Jul 1. doi: 10.1155/2020/6137083

PMCID:: PMC7349627

Abstract Article PDF–1.0M

Select item 72997295.

Identification of two novel mutations in POU4F3 gene associated with autosomal dominant hearing loss in Chinese families

Xiaohui Bai, Fengguo Zhang, Yun Xiao, Yu Jin, Qingyin Zheng, Haibo Wang, Lei Xu

J Cell Mol Med. 2020 Jun; 24(12): 6978–6987. Published online 2020 May 11. doi: 10.1111/jcmm.15359

PMCID:: PMC7299729

Abstract Article PDF–1.1M

Select item 59047946.

A Missense Mutation in POU4F3 Causes Midfrequency Hearing Loss in a Chinese ADNSHL Family

Xue Gao, Jin-Cao Xu, Wei-Qian Wang, Yong-Yi Yuan, Dan Bai, Sha-Sha Huang, Guo-Jian Wang, Yu Su, Jia Li, Dong-Yang Kang, Mei-Guang Zhang, Xi Lin, Pu Dai

Biomed Res Int. 2018; 2018: 5370802. Published online 2018 Apr 4. doi: 10.1155/2018/5370802

PMCID:: PMC5904794

Abstract Article PDF–1.0M

Select item 54352237.

POU4F3 mutation screening in Japanese hearing loss patients: Massively parallel DNA sequencing-based analysis identified novel variants associated with autosomal dominant hearing loss

Tomohiro Kitano, Maiko Miyagawa, Shin-ya Nishio, Hideaki Moteki, Kiyoshi Oda, Kenji Ohyama, Hiromitsu Miyazaki, Hiroshi Hidaka, Ken-ichi Nakamura, Takaaki Murata, Rina Matsuoka, Yoko Ohta, Nobuhiro Nishiyama, Kozo Kumakawa, Sakiko Furutate, Satoshi Iwasaki, Takechiyo Yamada, Yumi Ohta, Natsumi Uehara, Yoshihiro Noguchi, Shin-ichi Usami

PLoS One. 2017; 12(5): e0177636. Published online 2017 May 17. doi: 10.1371/journal.pone.0177636

PMCID:: PMC5435223

Abstract Article PDF–2.7M

Select item 51783748.

Mutation in the Hair Cell Specific Gene POU4F3 Is a Common Cause for Autosomal Dominant Nonsyndromic Hearing Loss in Chinese Hans

Longxia He, Xiuhong Pang, Penghui Chen, Hao Wu, Tao Yang

Neural Plast. 2016; 2016: 9890827. Published online 2016 Dec 8. doi: 10.1155/2016/9890827

PMCID:: PMC5178374

Abstract Article PDF–1023K

Select item 51437119.

A Novel Nonsense Mutation of POU4F3 Gene Causes Autosomal Dominant Hearing Loss

Chi Zhang, Mingming Wang, Yun Xiao, Fengguo Zhang, Yicui Zhou, Jianfeng Li, Qingyin Zheng, Xiaohui Bai, Haibo Wang

Neural Plast. 2016; 2016: 1512831. Published online 2016 Nov 24. doi: 10.1155/2016/1512831

Correction in:: Neural Plast. 2017; 2017: 9202847.

PMCID:: PMC5143711

Abstract Article PDF–1.8M

Select item 383251410.

SNP Linkage Analysis and Whole Exome Sequencing Identify a Novel POU4F3 Mutation in Autosomal Dominant Late-Onset Nonsyndromic Hearing Loss (DFNA15)

Hee-Jin Kim, Hong-Hee Won, Kyoung-Jin Park, Sung Hwa Hong, Chang-Seok Ki, Sang Sun Cho, Hanka Venselaar, Gert Vriend, Jong-Won Kim

PLoS One. 2013; 8(11): e79063. Published online 2013 Nov 18. doi: 10.1371/journal.pone.0079063

PMCID:: PMC3832514

Abstract Article PDF–942K

Select item 245378311.

Missense Mutations in POU4F3 Cause Autosomal Dominant Hearing Impairment DFNA15 and Affect Subcellular Localization and DNA Binding

Rob W.J. Collin, Ramesh Chellappa, Robert-Jan Pauw, Gert Vriend, Jaap Oostrik, Wendy van Drunen, Patrick L. Huygen, Ronald Admiraal, Lies H. Hoefsloot, Frans P.M. Cremers, Mengqing Xiang, Cor W.R.J. Cremers, Hannie Kremer

Hum Mutat. Author manuscript; available in PMC 2009 Apr 1.

Published in final edited form as: Hum Mutat. 2008 Apr; 29(4): 545–554. doi: 10.1002/humu.20693

PMCID:: PMC2453783

Abstract Article PDF–519K

Select item 26238512.

The DFNA15 Deafness Mutation Affects POU4F3 Protein Stability, Localization, and Transcriptional Activity

Sigal Weiss, Irit Gottfried, Itay Mayrose, Suvarna L. Khare, Mengqing Xiang, Sally J. Dawson, Karen B. Avraham

Mol Cell Biol. 2003 Nov; 23(22): 7957–7964. doi: 10.1128/MCB.23.22.7957-7964.2003

PMCID:: PMC262385

Abstract Article PDF–498K

Select item 554890113.

A novel missense variant in the nuclear localization signal of POU4F3 causes autosomal dominant non-syndromic hearing loss

Yin-Hung Lin, Yi-Hsin Lin, Ying-Chang Lu, Tien-Chen Liu, Chien-Yu Chen, Chuan-Jen Hsu, Pei-Lung Chen, Chen-Chi Wu

Sci Rep. 2017; 7: 7551. Published online 2017 Aug 8. doi: 10.1038/s41598-017-08236-y

PMCID:: PMC5548901

Abstract Article PDF–2.2M

Select item 492401814.

Genetic Variation in POU4F3 and GRHL2 Associated with Noise-Induced Hearing Loss in Chinese Population: A Case-Control Study

Xiangrong Xu, Qiuyue Yang, Jie Jiao, Lihua He, Shanfa Yu, Jingjing Wang, Guizhen Gu, Guoshun Chen, Wenhui Zhou, Hui Wu, Yanhong Li, Huanling Zhang

Int J Environ Res Public Health. 2016 Jun; 13(6): 561. Published online 2016 Jun 3. doi: 10.3390/ijerph13060561

PMCID:: PMC4924018

Abstract Article PDF–307K

Select item 429131115.

TRANSCRIPTION FACTORS WITH CONSERVED BINDING SITES NEAR ATOH1 ON THE POU4F3 GENE ENHANCE THE INDUCTION OF COCHLEAR HAIR CELLS

Ryoukichi Ikeda, Kwang Pak, Eduardo Chavez, Allen F. Ryan

Mol Neurobiol. Author manuscript; available in PMC 2016 Apr 1.

Published in final edited form as: Mol Neurobiol. 2015 Apr; 51(2): 672–684. doi: 10.1007/s12035-014-8801-y

PMCID:: PMC4291311

Abstract Article PDF–1.4M

Select item 483378716.

Genetics of vestibular disorders: pathophysiological insights

Lidia Frejo, Ina Giegling, Roberto Teggi, Jose A. Lopez-Escamez, Dan Rujescu

J Neurol. 2016; 263: 45–53. Published online 2016 Apr 15. doi: 10.1007/s00415-015-7988-9

PMCID:: PMC4833787

Abstract Article PDF–435K

Select item 422128217.

Regulation of the Orphan Nuclear Receptor Nr2f2 by the DFNA15 Deafness Gene Pou4f3

Chrysostomos Tornari, Emily R. Towers, Jonathan E. Gale, Sally J. Dawson

PLoS One. 2014; 9(11): e112247. Published online 2014 Nov 5. doi: 10.1371/journal.pone.0112247

PMCID:: PMC4221282

Abstract Article PDF–8.4M

Select item 657790418.

The Brn-3 family of POU-domain factors: primary structure, binding specificity, and expression in subsets of retinal ganglion cells and somatosensory neurons

M Xiang, L Zhou, JP Macke, T Yoshioka, SH Hendry, RL Eddy, TB Shows, J Nathans

J Neurosci. 1995 Jul 1; 15(7): 4762–4785. doi: 10.1523/JNEUROSCI.15-07-04762.1995

PMCID:: PMC6577904

Abstract PDF–21M

Select item 369240919.

RIT2, a neuron-specific small guanosine triphosphatase, is expressed in retinal neuronal cells and its promoter is modulated by the POU4 transcription factors

Ling Zhang, Karl Wahlin, Yuanyuan Li, Tomohiro Masuda, Zhiyong Yang, Donald J. Zack, Noriko Esumi

Mol Vis. 2013; 19: 1371–1386. Published online 2013 Jun 17.

PMCID:: PMC3692409

Abstract Article PDF–5.8M

Select item 533762120.

Aurora kinase A regulates Survivin stability through targeting FBXL7 in gastric cancer drug resistance and prognosis

M Kamran, Z-J Long, D Xu, S-S Lv, B Liu, C-L Wang, J Xu, E W-F Lam, Q Liu

Oncogenesis. 2017 Feb; 6(2): e298. Published online 2017 Feb 20. doi: 10.1038/oncsis.2016.80

PMCID:: PMC5337621

Abstract Article PDF–2.8M

PMC

Result Filters

Article attributes

Text availability

Publication date

Custom date range

Research Funder

Additional filters

Display Settings:

Send to:

Links from Gene

Items: 1 to 20 of 27

Display Settings:

Send to:

Supplemental Content

Find related data

Recent activity